File:Cyclohexane ring flip and relative conformation energies.svg
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[edit]DescriptionCyclohexane ring flip and relative conformation energies.svg |
English: Cyclohexane chair flip (ring inversion) reaction. Structures of the significant conformations (A, B, C & D) of the reaction are shown & plotted against their energy differences (not total energies). Inversion happens quickly & constantly in room temperature.
Conformations: A: chair B: twist-boat C: boat D: half-chair Valleys of the pink graph are conformations lowest in energy (shown as A & B). Peaks are conformations highest in energy (shown as C & D). Energies are A<B<C<D with D highest & A lowest in energy. A is thus the most stable conformation &, of all the other conformations, occurs most often in room temperature. Valleys A & B are local energy minima & A is global minima. A & B can thus be classified as conformers. Peaks are not conformers. Energy differences are mostly caused by anglular strain. Source for conformer classification:
Source for the relative energy differences & other info in this description:
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Date | |
Source | Own work |
Author | Keministi |
SVG development InfoField | This chemical equation was created with an unknown SVG tool. |
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[edit]Public domainPublic domainfalsefalse |
This image of a simple chemical equation is ineligible for copyright and therefore in the public domain, because it consists entirely of information that is common property and contains no original authorship. |
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